Hereditary spastic paraplegia
General Information (adopted from Orphanet):
| Synonyms, Signs: |
SPG HSP Strümpell-Lorrain disease Hereditary spastic paraparesis Familial spastic paraplegia |
| Number of Symptoms | 0 |
| OrphanetNr: | 685 |
| OMIM Id: |
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| ICD-10: |
G11.4 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | 5 [Orphanet] |
| Inheritance: |
X-linked recessive Autosomal recessive Autosomal dominant X-linked [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic neurodegenerative disease
-Rare genetic disease Rare neurodegenerative disease -Rare neurologic disease |
Comment:
| This term does not characterize a disease but a group of diseases. Annotations can be found at a more specific level. |
Symptom Information:
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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